Difference between revisions of "Part:BBa K1331001"

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It includes the whole coding sequence and a part of downstream noncoding sequence of rhlA.  
 
It includes the whole coding sequence and a part of downstream noncoding sequence of rhlA.  
 
The coding sequence of our part is similar with [[Part:BBa_K317998]][https://parts.igem.org/Part:BBa_K317998] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.
 
The coding sequence of our part is similar with [[Part:BBa_K317998]][https://parts.igem.org/Part:BBa_K317998] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.
 
  
 
===Usage and Biology===
 
===Usage and Biology===
 
RhlA together with rhlB encodes rhamnosyltransferase I for mono-rhamnolipids biosynthesis in ''Pseudomonas aeruginosa''.
 
RhlA together with rhlB encodes rhamnosyltransferase I for mono-rhamnolipids biosynthesis in ''Pseudomonas aeruginosa''.
 +
  
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 11:42, 17 October 2014

Modified rhlA coding sequence from Pseudomonas aeruginosa SQ6

This part encodes rhamnosyltransferase I subunit A. It includes the whole coding sequence and a part of downstream noncoding sequence of rhlA. The coding sequence of our part is similar with Part:BBa_K317998[1] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.

Usage and Biology

RhlA together with rhlB encodes rhamnosyltransferase I for mono-rhamnolipids biosynthesis in Pseudomonas aeruginosa.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 69
    Illegal BamHI site found at 629
    Illegal XhoI site found at 805
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 294
    Illegal BsaI.rc site found at 478